Chuanbiao Zhang, Kai Wu, Yiqun Wang, Mingzhe Shao, Jianjun Wang, Yanting Wang, Ming Li, Xin Zhou
{"title":"Accessing Ice–Water Interfaces with Critical Curvature for Investigating Ice Nucleation at Low Supercooling","authors":"Chuanbiao Zhang, Kai Wu, Yiqun Wang, Mingzhe Shao, Jianjun Wang, Yanting Wang, Ming Li, Xin Zhou","doi":"10.1021/acs.jctc.6c01371","DOIUrl":null,"url":null,"abstract":"<p>Formation of critical nuclei is the essential step of\r\nfirst-order\r\nphase transitions such as the crystallization of supercooled water.\r\nHowever, probing these nanometer-sized critical nuclei remains extremely\r\nchallenging in both experiments and simulations because they form\r\nrarely and exist transiently. Here we introduce a general simulation\r\napproach, also amenable to experimental realization, that enables\r\nspatiotemporally controlled formation and long-term stabilization\r\nof critical-sized ice nuclei. By covering a crystalline ice substrate\r\nwith graphene membranes containing a single nanopore, we show that\r\na spherical-cap ice nucleus forms barrierlessly on the nanopore and\r\ncoexists with supercooled water over macroscopic time scales at temperatures\r\nabove a pore-size-dependent threshold but rapidly grows once the temperature\r\nfalls below this threshold. The resulting (meta)stable ice–water\r\ninterface provides direct access to the thermodynamic and kinetic\r\nproperties of critical ice nuclei, allowing the critical radius, interfacial\r\nfree energy, molecular attachment rate, and nucleation rate to be\r\ndetermined using standard, unbiased simulations without any additional\r\nrare-event sampling. Beyond simulations, our results suggest a feasible\r\nexperimental strategy for directly probing stabilized critical nuclei\r\nand their associated ice–water interfaces at low supercooling\r\nconditions that are otherwise difficult to access. This framework\r\novercomes a long-standing barrier in both simulation and experimental\r\nstudies of ice nucleation and is readily extendable to other first-order\r\nphase-transition processes.</p>","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":"22 19","pages":"9992–10000"},"PeriodicalIF":5.8000,"publicationDate":"2026-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Theory and Computation","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jctc.6c01371","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Formation of critical nuclei is the essential step of
first-order
phase transitions such as the crystallization of supercooled water.
However, probing these nanometer-sized critical nuclei remains extremely
challenging in both experiments and simulations because they form
rarely and exist transiently. Here we introduce a general simulation
approach, also amenable to experimental realization, that enables
spatiotemporally controlled formation and long-term stabilization
of critical-sized ice nuclei. By covering a crystalline ice substrate
with graphene membranes containing a single nanopore, we show that
a spherical-cap ice nucleus forms barrierlessly on the nanopore and
coexists with supercooled water over macroscopic time scales at temperatures
above a pore-size-dependent threshold but rapidly grows once the temperature
falls below this threshold. The resulting (meta)stable ice–water
interface provides direct access to the thermodynamic and kinetic
properties of critical ice nuclei, allowing the critical radius, interfacial
free energy, molecular attachment rate, and nucleation rate to be
determined using standard, unbiased simulations without any additional
rare-event sampling. Beyond simulations, our results suggest a feasible
experimental strategy for directly probing stabilized critical nuclei
and their associated ice–water interfaces at low supercooling
conditions that are otherwise difficult to access. This framework
overcomes a long-standing barrier in both simulation and experimental
studies of ice nucleation and is readily extendable to other first-order
phase-transition processes.
期刊介绍:
The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.